Climate change, food security and health in Kiribati: a narrative review of the literature von Cauchi, John P., Correa-Velez, Ignacio, Bambrick, Hilary

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Joint effect of heat and air pollution on mortality in 620 cities of 36 countries von Stafoggia, Massimo, Michelozzi, Paola, Schneider, Alexandra, Armstrong, Ben, Scortichini, Matteo, Rai, Masna, Achilleos, Souzana, Alahmad, Barrak, Analitis, Antonis, Åström, Christofer, Bell, Michelle L, Calleja, Neville, Krage Carlsen, Hanne, Carrasco, Gabriel, Paul Cauchi, John, Dszs Coelho, Micheline, Correa, Patricia M, Diaz, Magali H, Entezari, Alireza, Forsberg, Bertil, Garland, Rebecca M, Leon Guo, Yue, Guo, Yuming, Hashizume, Masahiro, Holobaca, Iulian H, Íñiguez, Carmen, Jaakkola, Jouni J K, Kan, Haidong, Katsouyanni, Klea, Kim, Ho, Kyselý, Jan, Lavigne, Eric, Lee, Whanhee, Li, Shanshan, Maasikmets, Marek, Madureira, Joana, Mayvaneh, Fatemeh, Fook Sheng Ng, Chris, Nunes, Baltazar, Orru, Hans, V Ortega, Nicolás, Osorio, Samuel, Palomares, Alfonso D L, Pan, Shih-Chun, Pascal, Mathilde, Ragettli, Martina S, Rao, Shilpa, Raz, Raanan, Roye, Dominic, Ryti, Niilo, Hn Saldiva, Paulo, Samoli, Evangelia, Schwartz, Joel, Scovronick, Noah, Sera, Francesco, Tobias, Aurelio, Tong, Shilu, Dlc Valencia, César, Maria Vicedo-Cabrera, Ana, Urban, Aleš, Gasparrini, Antonio, Breitner, Susanne, De' Donato, Francesca K

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Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis von Zhang, Sai, Cooper-Knock, Johnathan, Weimer, Annika K., Shi, Minyi, Moll, Tobias, Marshall, Jack N.G., Harvey, Calum, Nezhad, Helia Ghahremani, Franklin, John, Souza, Cleide dos Santos, Ning, Ke, Wang, Cheng, Li, Jingjing, Dilliott, Allison A., Farhan, Sali, Elhaik, Eran, Pasniceanu, Iris, Livesey, Matthew R., Eitan, Chen, Hornstein, Eran, Kenna, Kevin P., Blair, Ian, Wray, Naomi R., Kiernan, Matthew, Mitne Neto, Miguel, Chio, Adriano, Cauchi, Ruben, Robberecht, Wim, van Damme, Philip, Corcia, Philippe, Couratier, Philippe, Hardiman, Orla, McLaughin, Russell, Gotkine, Marc, Drory, Vivian, Ticozzi, Nicola, Silani, Vincenzo, Veldink, Jan H., van den Berg, Leonard H., de Carvalho, Mamede, Mora Pardina, Jesus S., Povedano, Monica, Andersen, Peter, Weber, Markus, Başak, Nazli A., Al-Chalabi, Ammar, Shaw, Chris, Shaw, Pamela J., Morrison, Karen E., Landers, John E., Glass, Jonathan D., Veldink, Jan H., Ferraiuolo, Laura, Shaw, Pamela J., Snyder, Michael P.

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Association of Cardiometabolic Multimorbidity With Mortality von Di Angelantonio, Emanuele, Kaptoge, Stephen, Wormser, David, Willeit, Peter, Butterworth, Adam S, Bansal, Narinder, O’Keeffe, Linda M, Gao, Pei, Wood, Angela M, Burgess, Stephen, Freitag, Daniel F, Pennells, Lisa, Peters, Sanne A, Hart, Carole L, Håheim, Lise Lund, Gillum, Richard F, Nordestgaard, Børge G, Psaty, Bruce M, Yeap, Bu B, Knuiman, Matthew W, Nietert, Paul J, Kauhanen, Jussi, Salonen, Jukka T, Kuller, Lewis H, Simons, Leon A, van der Schouw, Yvonne T, Barrett-Connor, Elizabeth, Selmer, Randi, Crespo, Carlos J, Rodriguez, Beatriz, Verschuren, W. M. Monique, Salomaa, Veikko, Svärdsudd, Kurt, van der Harst, Pim, Björkelund, Cecilia, Wilhelmsen, Lars, Wallace, Robert B, Brenner, Hermann, Amouyel, Philippe, Barr, Elizabeth L. M, Iso, Hiroyasu, Onat, Altan, Trevisan, Maurizio, D'Agostino, Ralph B, Cooper, Cyrus, Kavousi, Maryam, Welin, Lennart, Roussel, Ronan, Hu, Frank B, Sato, Shinichi, Davidson, Karina W, Howard, Barbara V, Leening, Maarten J. G, Rosengren, Annika, Dörr, Marcus, Deeg, Dorly J. H, Kiechl, Stefan, Stehouwer, Coen D. A, Nissinen, Aulikki, Giampaoli, Simona, Donfrancesco, Chiara, Kromhout, Daan, Price, Jackie F, Peters, Annette, Meade, Tom W, Casiglia, Edoardo, Lawlor, Debbie A, Gallacher, John, Nagel, Dorothea, Franco, Oscar H, Assmann, Gerd, Dagenais, Gilles R, Jukema, J. Wouter, Sundström, Johan, Woodward, Mark, Brunner, Eric J, Khaw, Kay-Tee, Wareham, Nicholas J, Whitsel, Eric A, Njølstad, Inger, Hedblad, Bo, Wassertheil-Smoller, Sylvia, Engström, Gunnar, Rosamond, Wayne D, Selvin, Elizabeth, Sattar, Naveed, Thompson, Simon G, Danesh, John

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Analysis of volatile organic compounds of bacterial origin in chronic gastrointestinal diseases von Walton, Christopher, Fowler, Dawn P, Turner, Claire, Jia, Wenjing, Whitehead, Rebekah N, Griffiths, Lesley, Dawson, Claire, Waring, Rosemary H, Ramsden, David B, Cole, Jeffrey A, Cauchi, Michael, Bessant, Conrad, Hunter, John O

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci von Reschen, Michael E, Mahajan, Anubha, William Rayner, N, Scott, Laura J, Yengo, Loic, Wahl, Simone, Kestler, Hans, Chheda, Himanshu, Eisele, Lewin, Steinthorsdottir, Valgerdur, Chen, Han, Fuchsberger, Christian, Kwan, Phoenix, Thomsen, Soren K, Rundle, Jana K, van de Bunt, Martijn, Voight, Benjamin F, Abecasis, Gonçalo R, Baldassarre, Damiano, Carey, Jason, Chines, Peter S, Crenshaw, Andrew T, Edkins, Sarah, Eury, Elodie, Fontanillas, Pierre, Franks, Paul W, Gertow, Karl, Groves, Christopher J, Hassinen, Maija, Herder, Christian, Hreidarsson, Astradur B, Jackson, Anne U, Jonsson, Anna, Jørgensen, Marit E, Jørgensen, Torben, Kao, Wen-Hong L, Kerrison, Nicola D, Kinnunen, Leena, Kravic, Jasmina, Langford, Cordelia, Lichtner, Peter, Lindholm, Eero, Lobbens, Stéphane, Luan, Jian'an, Meyer, Julia, Mihailov, Evelin, Mühleisen, Thomas W, Navarro, Carmen, Oskolkov, Nikolay N, Pechlivanis, Sonali, Platou, Carl G P, Rybin, Denis, van der Schouw, Yvonne T, Sennblad, Bengt, Steinbach, Gerald, Storm, Petter, Sun, Qi, Thorand, Barbara, Tikkanen, Emmi, Trakalo, Joseph, Tremoli, Elena, Wood, Andrew R, Zeggini, Eleftheria, Birney, Ewan, Pasquali, Lorenzo, Pankow, James S, van Duijn, Cornelia, Sijbrands, Eric, Hu, Frank B, Thorsteinsdottir, Unnur, Stefansson, Kari, Lakka, Timo A, Rauramaa, Rainer, Stumvoll, Michael, Korpi-Hyövälti, Eeva, Kuusisto, Johanna, Metspalu, Andres, Jöcke, Karl-Heinz, Moebus, Susanne, Bergman, Richard N, Collins, Francis S, Mohlke, Karen L, Koistinen, Heikki, Tuomilehto, Jaakko, Deloukas, Panagiotis, Donnelly, Peter J, Frayling, Timothy M, Sladek, Rob, Froguel, Philippe, Hansen, Torben, Kathiresan, Sekar, Barroso, Inês, Langenberg, Claudia, Wareham, Nicholas J, O'Callaghan, Christopher A, Gloyn, Anna L, Altshuler, David, Boehnke, Michael, Teslovich, Tanya M, Morris, Andrew P

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Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene von Cooper-Knock, Johnathan, Zhang, Sai, Kenna, Kevin P., Moll, Tobias, Franklin, John P., Allen, Samantha, Nezhad, Helia Ghahremani, Iacoangeli, Alfredo, Yacovzada, Nancy Y., Eitan, Chen, Hornstein, Eran, Elhaik, Eran, Celadova, Petra, Bose, Daniel, Farhan, Sali, Fishilevich, Simon, Lancet, Doron, Morrison, Karen E., Shaw, Christopher E., Al-Chalabi, Ammar, Blair, Ian, Wray, Naomi, Kiernan, Matthew, Neto, Miguel Mitne, Chio, Adriano, Cauchi, Ruben, Robberecht, Wim, van Damme, Philip, Corcia, Phillippe, Couratier, Phillipe, Hardiman, Orla, McLaughlin, Russel, Gotkine, Marc, Drory, Vivan, Ticozzi, Nicola, Silani, Vincenzo, Veldink, Jan, van den Berg, Leonard, de Carvalho, Mamede, Pardina, Jesus Mora, Povedano, Monica, Andersen, Peter, Wber, Markus, Başak, Nazli, Al-Chalabi, Ammar, Shaw, Christopher, Shaw, Pamela, Morrison, Karen, Landers, John, Glass, Jonathan, Veldink, Jan H., Kirby, Janine, Snyder, Michael P., Shaw, Pamela J.

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Computing linkage disequilibrium aware genome embeddings using autoencoders von Taş, Gizem, Westerdijk, Timo, Postma, Eric, Veldink, Jan H, Schönhuth, Alexander, Balvert, Marleen

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Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS von Hop, Paul J, Zwamborn, Ramona A.J, Hannon, Eilis, Shireby, Gemma L, Nabais, Marta F, Walker, Emma M, van Rheenen, Wouter, van Vugt, Joke J.F.A, Dekker, Annelot M, Westeneng, Henk-Jan, Tazelaar, Gijs H.P, van Eijk, Kristel R, Moisse, Matthieu, Baird, Denis, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Ticozzi, Nicola, Ratti, Antonia, Cooper-Knock, Jonathan, Morrison, Karen E, Shaw, Pamela J, Basak, A. Nazli, Chio, Adriano, Calvo, Andrea, Moglia, Cristina, Canosa, Antonio, Brunetti, Maura, Grassano, Maurizio, Gotkine, Marc, Lerner, Yossef, Zabari, Michal, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Pardina, Jesus S. Mora, Salas, Teresa, Dion, Patrick, Ross, Jay P, Henderson, Robert D, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Nicholson, Garth, Rowe, Dominic B, Pamphlett, Roger, Mather, Karen A, Sachdev, Perminder S, Furlong, Sarah, Garton, Fleur C, Henders, Anjali K, Lin, Tian, Ngo, Shyuan T, Steyn, Frederik J, Wallace, Leanne, Williams, Kelly L, Neto, Miguel Mitne, Cauchi, Ruben J, Blair, Ian P, Kiernan, Matthew C, Drory, Vivian, Povedano, Monica, de Carvalho, Mamede, Pinto, Susana, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Landers, John E, Shaw, Christopher E, Andersen, Peter M, McRae, Allan F, van Es, Michael A, Pasterkamp, R. Jeroen, Wray, Naomi R, McLaughlin, Russell L, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Al-Chalabi, Ammar, van den Berg, Leonard H, Van Damme, Philip, Mill, Jonathan, Veldink, Jan H

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Fibroblast growth factor receptors and their ligands in the adult rat kidney von Cancilla, Belinda, Davies, Ann, Cauchi, Jennifer A., Risbridger, Gail P., Bertram, John F.

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Low-Frequency Variants in HMGA1 Are Not Associated With Type 2 Diabetes Risk von MARQUEZ, Marcel, HUYVAERT, Marlene, PATTOU, Francois, POULAIN-GODEFROY, Odile, CHARPENTIER, Guillaume, CARLSSON, Lena M. S, JACOBSON, Peter, SJÖSTRÖM, Lars, LANTIERI, Olivier, HEUDE, Barbara, WALLEY, Andrew, BALKAU, Beverley, PERRY, John R. B, MARRE, Michel, FROGUEL, Philippe, CAUCHI, Stephane, PEARSON, Richard D, FALCHI, Mario, MORRIS, Andrew P, VIVEQUIN, Sidonie, LOBBENS, Stephane, YENGO, Loic, GAGET, Stefan

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Vitreous relapse following primary chemotherapy for retinoblastoma: is adjuvant diode laser a risk factor? von Gombos, D S, Cauchi, P A, Hungerford, J L, Addison, P, Coen, P G, Kingston, J E

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Application of gas chromatography mass spectrometry (GC–MS) in conjunction with multivariate classification for the diagnosis of gastrointestinal diseases von Cauchi, Michael, Fowler, Dawn P., Walton, Christopher, Turner, Claire, Jia, Wenjing, Whitehead, Rebekah N., Griffiths, Lesley, Dawson, Claire, Bai, Hao, Waring, Rosemary H., Ramsden, David B., Hunter, John O., Cole, Jeffrey A., Bessant, Conrad

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Diversity and distribution of sulphate-reducing bacteria in human faeces from healthy subjects and patients with inflammatory bowel disease von Jia, Wenjing, Whitehead, Rebekah N., Griffiths, Lesley, Dawson, Claire, Bai, Hao, Waring, Rosemary H., Ramsden, David B., Hunter, John O., Cauchi, Michael, Bessant, Conrad, Fowler, Dawn P., Walton, Christopher, Turner, Claire, Cole, Jeffrey A.

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Molecular characterization of Camberwell virus and sequence variation in ORF3 of small round-structured (Norwalk-like) viruses von Cauchi, Mark R., Doultree, Jennifer C., Marshall, John A., Wright, Peter J.

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Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases von Perry, John R. B, Voight, Benjamin F, Yengo, Loïc, Amin, Najaf, Dupuis, Josée, Ganser, Martha, Grallert, Harald, Navarro, Pau, Li, Man, Steinthorsdottir, Valgerdur, Almgren, Peter, Arking, Dan E, Aulchenko, Yurii, Balkau, Beverley, Benediktsson, Rafn, Bergman, Richard N, Boerwinkle, Eric, Bonnycastle, Lori, Burtt, Noël P, Campbell, Harry, Charpentier, Guillaume, Collins, Francis S, Gieger, Christian, Green, Todd, Hadjadj, Samy, Hattersley, Andrew T, Herder, Christian, Kottgen, Anna, Labrune, Yann, Langenberg, Claudia, Mohlke, Karen L, Morris, Andrew P, Oostra, Ben, Pankow, James, Petersen, Ann-Kristin, Pramstaller, Peter P, Prokopenko, Inga, Rathmann, Wolfgang, Rayner, William, Roden, Michael, Rudan, Igor, Rybin, Denis, Sigurdsson, Gunnar, Sladek, Rob, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Tuomilehto, Jaakko, Uitterlinden, Andre G, Vivequin, Sidonie, Weedon, Michael N, Wright, Alan F, Illig, Thomas, Kao, Linda, Wilson, James F, Stefansson, Kari, van Duijn, Cornelia, Altschuler, David, Morris, Andrew D, Boehnke, Michael, McCarthy, Mark I, Froguel, Philippe, Palmer, Colin N. A, Wareham, Nicholas J, Groop, Leif, Frayling, Timothy M, Cauchi, Stéphane, Qi, Lu, Scott, Robert A, Hofman, Albert, Johnson, Andrew D, Kraft, Peter, Manning, Alisa K, Scott, Laura J, Hu, Frank B, Meigs, James Benjamin

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Van Deerlin, Vivianna, Roediger, Annekathrin, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Williams, Kelly, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan, Universitat Autònoma de Barcelona

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Roediger, Annekathrin, Gaur, Nayana, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Gaunt, Tom, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan H, Universitat Autònoma de Barcelona

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Author Correction : Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biol... von Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Van Deerlin, Vivianna, Roediger, Annekathrin, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Williams, Kelly, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan, Universitat Autònoma de Barcelona

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Author Correction : Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biol... von Hop, Paul J, Bakker, Olivier B, Baird, Denis, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Kooyman, Maarten, Byrne, Ross P, Heverin, Mark, Al Khleifat, Ahmad, Ticozzi, Nicola, Cooper-Knock, Johnathan, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Orrell, Richard W, van der Kooi, Anneke J, Fogh, Isabella, Gellera, Cinzia, Corti, Stefania, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Grassano, Maurizio, Pupillo, Elisabetta, Logroscino, Giancarlo, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Meininger, Vincent, Salachas, François, Assialioui, Abdelilah, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Kraft, Julia, Hofman, Albert, Cichon, Sven, Nöthen, Markus M, Traynor, Bryan J, Singleton, Andrew B, Wiedau-Pazos, Martina, Roediger, Annekathrin, Gaur, Nayana, Stubendorff, Beatrice, Graff, Caroline, Brylev, Lev, Zidar, Janez, Ravnik-Glavač, Metka, Glavač, Damjan, Drory, Vivian, Povedano, Monica, Furlong, Sarah, Mathers, Susan, McCombe, Pamela A, Needham, Merrilee, Rowe, Dominic B, Henders, Anjali K, Weber, Markus, Rouleau, Guy A, Silani, Vincenzo, Glass, Jonathan D, Brown, Robert H, Landers, John E, Andersen, Peter Munch, Groen, Ewout J. N, Fan, Dongsheng, McRae, Allan F, Gaunt, Tom, Hardiman, Orla, Kenna, Kevin P, Tsai, Ellen, Runz, Heiko, Franke, Lude, van den Berg, Leonard H, Veldink, Jan H, Universitat Autònoma de Barcelona

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